Your browser doesn't support javascript.
loading
Orphan receptor IL-17RD regulates Toll-like receptor signalling via SEFIR/TIR interactions.
Mellett, Mark; Atzei, Paola; Bergin, Ronan; Horgan, Alan; Floss, Thomas; Wurst, Wolfgang; Callanan, John J; Moynagh, Paul N.
Afiliação
  • Mellett M; Department of Biology, Institute of Immunology, National University of Ireland Maynooth, Maynooth, County Kildare, Ireland.
  • Atzei P; Department of Biology, Institute of Immunology, National University of Ireland Maynooth, Maynooth, County Kildare, Ireland.
  • Bergin R; Department of Biology, Institute of Immunology, National University of Ireland Maynooth, Maynooth, County Kildare, Ireland.
  • Horgan A; Department of Biology, Institute of Immunology, National University of Ireland Maynooth, Maynooth, County Kildare, Ireland.
  • Floss T; Helmholtz Zentrum München, Institute of Developmental Genetics, Munich, Neuherberg 85764, Germany.
  • Wurst W; Helmholtz Zentrum München, Institute of Developmental Genetics, Munich, Neuherberg 85764, Germany.
  • Callanan JJ; UCD School of Veterinary Medicine &Conway Institute of Biomolecular &Biomedical Research, UCD, Belfield, Dublin 4, Ireland.
  • Moynagh PN; 1] Department of Biology, Institute of Immunology, National University of Ireland Maynooth, Maynooth, County Kildare, Ireland [2] Centre for Infection and Immunity, School of Medicine, Dentistry and Biomedical Sciences, Queen's University Belfast, Belfast, Northern Ireland BT9 7AE, UK.
Nat Commun ; 6: 6669, 2015 Mar 26.
Article em En | MEDLINE | ID: mdl-25808990
ABSTRACT
Receptor families of the innate immune response engage in 'cross-talk' to tailor optimal immune responses against invading pathogens. However, these responses are subject to multiple levels of regulation to keep in check aberrant inflammatory signals. Here, we describe a role for the orphan receptor interleukin-17 receptor D (IL-17RD) in negatively regulating Toll-like receptor (TLR)-induced responses. Deficiency of IL-17RD expression in cells leads to enhanced pro-inflammatory signalling and gene expression in response to TLR stimulation, and Il17rd(-/-) mice are more susceptible to TLR-induced septic shock. We demonstrate that the intracellular Sef/IL-17R (SEFIR) domain of IL-17RD targets TIR adaptor proteins to inhibit TLR downstream signalling thus revealing a paradigm involving cross-regulation of members of the IL-17R and TLR families.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Choque Séptico / Regulação da Expressão Gênica / NF-kappa B / Receptores de Interleucina / Fatores Reguladores de Interferon / Receptores Toll-Like / Imunidade Inata Limite: Animals / Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Choque Séptico / Regulação da Expressão Gênica / NF-kappa B / Receptores de Interleucina / Fatores Reguladores de Interferon / Receptores Toll-Like / Imunidade Inata Limite: Animals / Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article